Colocalized neurotransmitters in the hindbrain cooperate in adaptation to chronic hypernatremia Article Swipe
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· 2020
· Open Access
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· DOI: https://doi.org/10.1007/s00429-020-02049-y
Chronic hypernatremia activates the central osmoregulatory mechanisms and inhibits the function of the hypothalamic–pituitary–adrenal (HPA) axis. Noradrenaline (NE) release into the periventricular anteroventral third ventricle region (AV3V), the supraoptic (SON) and hypothalamic paraventricular nuclei (PVN) from efferents of the caudal ventrolateral (cVLM) and dorsomedial (cDMM) medulla has been shown to be essential for the hypernatremia-evoked responses and for the HPA response to acute restraint. Notably, the medullary NE cell groups highly coexpress prolactin-releasing peptide (PrRP) and nesfatin-1/NUCB2 (nesfatin), therefore, we assumed they contributed to the reactions to chronic hypernatremia. To investigate this, we compared two models: homozygous Brattleboro rats with hereditary diabetes insipidus (DI) and Wistar rats subjected to chronic high salt solution (HS) intake. HS rats had higher plasma osmolality than DI rats. PrRP and nesfatin mRNA levels were higher in both models, in both medullary regions compared to controls. Elevated basal tyrosine hydroxylase (TH) expression and impaired restraint-induced TH, PrRP and nesfatin expression elevations in the cVLM were, however, detected only in HS, but not in DI rats. Simultaneously, only HS rats exhibited classical signs of chronic stress and severely blunted hormonal reactions to acute restraint. Data suggest that HPA axis responsiveness to restraint depends on the type of hypernatremia, and on NE capacity in the cVLM. Additionally, NE and PrRP signalization primarily of medullary origin is increased in the SON, PVN and AV3V in HS rats. This suggests a cooperative action in the adaptation responses and designates the AV3V as a new site for PrRP’s action in hypernatremia.
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- Type
- article
- Language
- en
- Landing Page
- https://doi.org/10.1007/s00429-020-02049-y
- https://link.springer.com/content/pdf/10.1007/s00429-020-02049-y.pdf
- OA Status
- hybrid
- Cited By
- 4
- References
- 81
- Related Works
- 10
- OpenAlex ID
- https://openalex.org/W3012872666
Raw OpenAlex JSON
- OpenAlex ID
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https://openalex.org/W3012872666Canonical identifier for this work in OpenAlex
- DOI
-
https://doi.org/10.1007/s00429-020-02049-yDigital Object Identifier
- Title
-
Colocalized neurotransmitters in the hindbrain cooperate in adaptation to chronic hypernatremiaWork title
- Type
-
articleOpenAlex work type
- Language
-
enPrimary language
- Publication year
-
2020Year of publication
- Publication date
-
2020-03-21Full publication date if available
- Authors
-
Rita Matuska, Dóra Zelena, Katalin Könczöl, Rege Sugárka Papp, Máté Durst, Dorina Guba, Bibiána Török, Péter Várnai, Zsuzsanna TóthList of authors in order
- Landing page
-
https://doi.org/10.1007/s00429-020-02049-yPublisher landing page
- PDF URL
-
https://link.springer.com/content/pdf/10.1007/s00429-020-02049-y.pdfDirect link to full text PDF
- Open access
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YesWhether a free full text is available
- OA status
-
hybridOpen access status per OpenAlex
- OA URL
-
https://link.springer.com/content/pdf/10.1007/s00429-020-02049-y.pdfDirect OA link when available
- Concepts
-
Hypernatremia, Internal medicine, Endocrinology, Diabetes insipidus, Posterior pituitary, Hypothalamus, Vasopressin, Osmoregulation, Medicine, Biology, Chemistry, Pituitary gland, Hormone, Ecology, Organic chemistry, Sodium, SalinityTop concepts (fields/topics) attached by OpenAlex
- Cited by
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4Total citation count in OpenAlex
- Citations by year (recent)
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2025: 2, 2024: 1, 2021: 1Per-year citation counts (last 5 years)
- References (count)
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81Number of works referenced by this work
- Related works (count)
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10Other works algorithmically related by OpenAlex
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| abstract_inverted_index.Notably, | 65 |
| abstract_inverted_index.PrRP’s | 248 |
| abstract_inverted_index.capacity | 206 |
| abstract_inverted_index.compared | 94, 139 |
| abstract_inverted_index.detected | 162 |
| abstract_inverted_index.diabetes | 102 |
| abstract_inverted_index.function | 11 |
| abstract_inverted_index.hormonal | 184 |
| abstract_inverted_index.however, | 161 |
| abstract_inverted_index.impaired | 149 |
| abstract_inverted_index.inhibits | 9 |
| abstract_inverted_index.nesfatin | 127, 154 |
| abstract_inverted_index.response | 61 |
| abstract_inverted_index.severely | 182 |
| abstract_inverted_index.solution | 113 |
| abstract_inverted_index.suggests | 231 |
| abstract_inverted_index.tyrosine | 144 |
| abstract_inverted_index.activates | 3 |
| abstract_inverted_index.classical | 176 |
| abstract_inverted_index.coexpress | 72 |
| abstract_inverted_index.controls. | 141 |
| abstract_inverted_index.efferents | 37 |
| abstract_inverted_index.essential | 52 |
| abstract_inverted_index.exhibited | 175 |
| abstract_inverted_index.increased | 220 |
| abstract_inverted_index.insipidus | 103 |
| abstract_inverted_index.medullary | 67, 137, 217 |
| abstract_inverted_index.primarily | 215 |
| abstract_inverted_index.reactions | 86, 185 |
| abstract_inverted_index.responses | 56, 238 |
| abstract_inverted_index.restraint | 196 |
| abstract_inverted_index.subjected | 108 |
| abstract_inverted_index.ventricle | 25 |
| abstract_inverted_index.adaptation | 237 |
| abstract_inverted_index.designates | 240 |
| abstract_inverted_index.elevations | 156 |
| abstract_inverted_index.expression | 147, 155 |
| abstract_inverted_index.hereditary | 101 |
| abstract_inverted_index.homozygous | 97 |
| abstract_inverted_index.mechanisms | 7 |
| abstract_inverted_index.osmolality | 121 |
| abstract_inverted_index.restraint. | 64, 188 |
| abstract_inverted_index.supraoptic | 29 |
| abstract_inverted_index.therefore, | 79 |
| abstract_inverted_index.(nesfatin), | 78 |
| abstract_inverted_index.Brattleboro | 98 |
| abstract_inverted_index.contributed | 83 |
| abstract_inverted_index.cooperative | 233 |
| abstract_inverted_index.dorsomedial | 44 |
| abstract_inverted_index.hydroxylase | 145 |
| abstract_inverted_index.investigate | 91 |
| abstract_inverted_index.hypothalamic | 32 |
| abstract_inverted_index.Additionally, | 210 |
| abstract_inverted_index.Noradrenaline | 17 |
| abstract_inverted_index.anteroventral | 23 |
| abstract_inverted_index.hypernatremia | 2 |
| abstract_inverted_index.signalization | 214 |
| abstract_inverted_index.ventrolateral | 41 |
| abstract_inverted_index.hypernatremia, | 202 |
| abstract_inverted_index.hypernatremia. | 89, 251 |
| abstract_inverted_index.osmoregulatory | 6 |
| abstract_inverted_index.responsiveness | 194 |
| abstract_inverted_index.Simultaneously, | 171 |
| abstract_inverted_index.paraventricular | 33 |
| abstract_inverted_index.periventricular | 22 |
| abstract_inverted_index.nesfatin-1/NUCB2 | 77 |
| abstract_inverted_index.restraint-induced | 150 |
| abstract_inverted_index.prolactin-releasing | 73 |
| abstract_inverted_index.hypernatremia-evoked | 55 |
| abstract_inverted_index.hypothalamic–pituitary–adrenal | 14 |
| cited_by_percentile_year.max | 97 |
| cited_by_percentile_year.min | 89 |
| countries_distinct_count | 1 |
| institutions_distinct_count | 9 |
| sustainable_development_goals[0].id | https://metadata.un.org/sdg/3 |
| sustainable_development_goals[0].score | 0.7400000095367432 |
| sustainable_development_goals[0].display_name | Good health and well-being |
| citation_normalized_percentile.value | 0.39215686 |
| citation_normalized_percentile.is_in_top_1_percent | False |
| citation_normalized_percentile.is_in_top_10_percent | False |